ClinVar Miner

Variants in gene DOLK with conflicting interpretations

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Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
405 54 0 8 17 0 1 23

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 0 1 1 0 0
likely pathogenic 1 0 1 0 0
uncertain significance 1 1 0 11 6
likely benign 0 0 11 0 7
benign 0 0 6 7 0

All variants with conflicting interpretations #

Total variants: 23
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014908.4(DOLK):c.-49A>G rs116439010 0.01852
NM_014908.4(DOLK):c.1dup (p.Met1fs) rs531969689 0.00573
NM_014908.4(DOLK):c.186G>A (p.Arg62=) rs148171062 0.00299
NM_014908.4(DOLK):c.631C>T (p.Arg211Cys) rs145310298 0.00238
NM_014908.4(DOLK):c.771C>T (p.Ile257=) rs147416890 0.00205
NM_014908.4(DOLK):c.1079A>G (p.Tyr360Cys) rs138453255 0.00111
NM_014908.4(DOLK):c.700A>G (p.Met234Val) rs139787271 0.00102
NM_014908.4(DOLK):c.671A>T (p.Asp224Val) rs17485436 0.00074
NM_014908.4(DOLK):c.873C>T (p.Leu291=) rs148646968 0.00073
NM_014908.4(DOLK):c.1314C>T (p.Leu438=) rs148118523 0.00071
NM_014908.4(DOLK):c.525T>G (p.Val175=) rs200278288 0.00045
NM_014908.4(DOLK):c.1450A>G (p.Ile484Val) rs147630977 0.00044
NM_014908.4(DOLK):c.1481A>G (p.Asp494Gly) rs145292760 0.00039
NM_014908.4(DOLK):c.1394G>A (p.Arg465His) rs148930043 0.00031
NM_014908.4(DOLK):c.1437T>C (p.Ser479=) rs574290806 0.00019
NM_014908.4(DOLK):c.579G>A (p.Glu193=) rs28365522 0.00017
NM_014908.4(DOLK):c.633C>T (p.Arg211=) rs147647278 0.00013
NM_014908.4(DOLK):c.1446G>A (p.Ala482=) rs201027607 0.00012
NM_014908.4(DOLK):c.192A>G (p.Leu64=) rs563156233 0.00009
NM_014908.4(DOLK):c.210C>G (p.Val70=) rs750368652 0.00006
NM_014908.4(DOLK):c.1011A>G (p.Arg337=) rs375939944 0.00005
NM_014908.4(DOLK):c.1558A>G (p.Thr520Ala) rs374860681 0.00005
NM_014908.4(DOLK):c.2T>C (p.Met1Thr) rs587777137

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